Biomaterials and Tissue Engineering Group, Leeds Dental Institute, University of Leeds, Leeds, LS2 9LU, UK.
Cell Tissue Res. 2013 Jun;352(3):495-507. doi: 10.1007/s00441-013-1586-x. Epub 2013 Mar 12.
A major clinical need exists for cartilage repair and regeneration. Despite many different strategies having been pursued, the identification of an optimised cell type and of pre-treatment conditions remains a challenge. This study compares the cartilage-like tissue generated by human bone marrow stromal cells (HBMSCs) and human neonatal and adult chondrocytes cultured on three-dimensional (3D) scaffolds under various conditions in vitro and in vivo with the aim of informing future cartilage repair strategies based upon tissue-engineering approaches. After 3 weeks in vitro culture, all three cell types showed cartilage-like tissue formation on 3D poly (lactide-co-glycolide) acid scaffolds only when cultured in chondrogenic medium. After 6 weeks of chondro-induction, neonatal chondrocyte constructs revealed the most cartilage-like tissue formation with a prominent superficial zone-like layer, a middle zone-like structure and the thinnest fibrous capsule. HBMSC constructs had the thickest fibrous capsule formation. Under basal culture conditions, neonatal articular chondrocytes failed to form any tissue, whereas HBMSCs and adult chondrocytes showed thick fibrous capsule formation at 6 weeks. After in vivo implantation, all groups generated more compact tissues compared with in vitro constructs. Pre-culturing in chondrogenic media for 1 week before implantation reduced fibrous tissue formation in all cell constructs at week 3. After 6 weeks, only the adult chondrocyte group pre-cultured in chondrogenic media was able to maintain a more chondrogenic/less fibrocartilaginous phenotype. Thus, pre-culture under chondrogenic conditions is required to maintain a long-term chondrogenic phenotype, with adult chondrocytes being a more promising cell source than HBMSCs for articular cartilage tissue engineering.
临床上急需进行软骨修复和再生。尽管已经采用了许多不同的策略,但确定最佳的细胞类型和预处理条件仍然是一个挑战。本研究比较了在体外和体内不同条件下,骨髓基质细胞(HBMSCs)和人新生儿及成体软骨细胞在三维(3D)支架上培养所产生的类软骨组织,旨在为基于组织工程方法的未来软骨修复策略提供信息。在体外培养 3 周后,所有三种细胞类型仅在软骨形成培养基中培养时,才能在 3D 聚(乳酸-共-乙醇酸)酸支架上形成类软骨组织。经过 6 周的软骨诱导,新生儿软骨细胞构建体显示出最多的类软骨组织形成,具有明显的浅层样层、中层样结构和最薄的纤维囊。HBMSC 构建体具有最厚的纤维囊形成。在基础培养条件下,新生儿关节软骨细胞无法形成任何组织,而 HBMSCs 和成年软骨细胞在 6 周时显示出厚的纤维囊形成。体内植入后,与体外构建体相比,所有组均生成更致密的组织。在植入前用软骨形成培养基预培养 1 周可减少所有细胞构建体中的纤维组织形成。6 周后,只有在软骨形成培养基中预培养的成体软骨细胞组能够维持更具软骨/少纤维软骨表型。因此,需要在软骨形成条件下进行预培养以维持长期的软骨形成表型,而成体软骨细胞比 HBMSCs 更适合用于关节软骨组织工程。